Nickel-catalyzed alkenylative cross-coupling reaction of alkyl sulfides

Kentaro Ishizuka, Hirofumi Seike, Takuji Hatakeyama, Masaharu Nakamura

Research output: Contribution to journalArticle

31 Citations (Scopus)

Abstract

A novel cross-coupling reaction of alkyl aryl sulfides with aryl Grignard reagents has been achieved to produce the alkenyl-aryl coupling products in high yields by using catalytic Ni(cod)2 and a bulky N-heterocyclic carbene ligand, SIPr.

Original languageEnglish
Pages (from-to)13117-13119
Number of pages3
JournalJournal of the American Chemical Society
Volume132
Issue number38
DOIs
Publication statusPublished - Sep 29 2010

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Gadiformes
Cross Reactions
Sulfides
Nickel
Ligands
carbene

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Chemistry(all)
  • Biochemistry
  • Colloid and Surface Chemistry

Cite this

Nickel-catalyzed alkenylative cross-coupling reaction of alkyl sulfides. / Ishizuka, Kentaro; Seike, Hirofumi; Hatakeyama, Takuji; Nakamura, Masaharu.

In: Journal of the American Chemical Society, Vol. 132, No. 38, 29.09.2010, p. 13117-13119.

Research output: Contribution to journalArticle

Ishizuka, Kentaro ; Seike, Hirofumi ; Hatakeyama, Takuji ; Nakamura, Masaharu. / Nickel-catalyzed alkenylative cross-coupling reaction of alkyl sulfides. In: Journal of the American Chemical Society. 2010 ; Vol. 132, No. 38. pp. 13117-13119.
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